Rearrangement of (substituted benzyl)trimethylammonium ylides in a nonbasic medium: the improved Sommelet-Hauser rearrangement
作者:Mitsuji Nakano、Yoshiro Sato
DOI:10.1021/jo00385a035
日期:1987.5
NAKANO MITSUJI; SATO YOSHIRO, J. ORG. CHEM., 52,(1987) N 9, 1844-1847
作者:NAKANO MITSUJI、 SATO YOSHIRO
DOI:——
日期:——
Selection of a Sommelet-Hauser or a Stevens rearrangement pathway of N,N-dimethyl(substituted benzyl)ammonium N-alkylides
作者:Tetsuya Tanaka、Naohiro Shirai、Junji Sugimori、Yoshiro Sato
DOI:10.1021/jo00044a050
日期:1992.8
A convenient synthesis of o-methylbenzylamine derivatives from benzyl halides: the improved Sommelet–Hauser rearrangement
作者:Mitsuji Nakano、Yoshiro Sato
DOI:10.1039/c39850001684
日期:——
Desilylation by fluoride anion of benzyldimethyl(trimethylsilylmethyl)ammonium halides having a Cl–, CN–, or AcO– substituent on the benzene ring gave high yields of the Sommelet–Hauserrearrangement products at room temperature.